Opsoclonus-myoclonus syndrome associated with herpes simplex encephalitis

Detalhes bibliográficos
Autor(a) principal: Afonso, C.O.M.
Data de Publicação: 2015
Outros Autores: Campos, M.L.S., Maia, Ferdinand Gilbert Saraiva da Silva, Campêlo, C.L.C., Camilo, A.F.C., Correia, Carlos Eduardo Rocha, Fernandes, José Veríssimo, Figueiredo, Marcelo Marinho de, Silva, R.A.
Tipo de documento: Artigo
Idioma: por
Título da fonte: Repositório Institucional da UFRN
Texto Completo: https://repositorio.ufrn.br/handle/123456789/52559
Resumo: Background: Opsoclonus-myoclonus ataxia is a rare neurologic syn drome, often paraneoplastic in origin, but reported in association with various infections. Little is known about adult-onset opsoclonus myoclonus syndrome (OMS) outside of individual case reports Objective: Describe a case of herpes-simplex virus 1 encephalitis presenting as opsoclonus-myoclonus ataxia Patients and methods: A 35 year-old woman, with no known comorbidities, developed a headache with nausea and vomiting, without fever or nuchal rigidity. In the following 48-hours, she presented an altered mental status, opsoclonus and myoclonus and was admitted to hospital. Lumbar puncture: 40 cells (60% mononu clear), protein 140 mg/dL and a normal glucose. Gram stain and culture for bacteria and fungi were negative. A PCR for herpes simplex virus was positive. Brain MRI: normal. Chest, Abdomen and Pelvis CT: no signs of neoplasia. Results: The patient received intra-venous acyclovir for 21 days, with resolution of symptoms Conclusion: OMS is an uncommon presentation of infections of central nervous system. Its fame extends further to the fact that OMS can be a harbinger of occult malignancy. The Adult-onset presentation is rare. Paraneoplastic and parainfectious causes (particularly virus) are common; however, more often OMS in adults occurs after systemic infection. After this report, HSV1 infection should be considered in OMS cases. We described the first case of OMS secondary to Herpes-Simplex Virus 1 infection.
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spelling Afonso, C.O.M.Campos, M.L.S.Maia, Ferdinand Gilbert Saraiva da SilvaCampêlo, C.L.C.Camilo, A.F.C.Correia, Carlos Eduardo RochaFernandes, José VeríssimoFigueiredo, Marcelo Marinho deSilva, R.A.2023-05-29T17:23:27Z2023-05-29T17:23:27Z2015-10-15CORREIA, Carlos Eduardo Rocha; et al. Opsoclonus-myoclonus syndrome associated with herpes simplex encephalitis. Journal Of The Neurological Sciences, [S.l.], v. 357, p. 56, out. 2015. Elsevier BV. Disponível em: https://www.sciencedirect.com/science/article/pii/S0022510X15007169?via%3Dihub. Acesso em: 29 mio 2023. DOI: http://dx.doi.org/10.1016/j.jns.2015.08.220https://repositorio.ufrn.br/handle/123456789/5255910.1016/j.jns.2015.08.220.Journal Of The Neurological Sciencesopsoclonus-myoclonusencephalitisparaneoplasticOpsoclonus-myoclonus syndrome associated with herpes simplex encephalitisinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleBackground: Opsoclonus-myoclonus ataxia is a rare neurologic syn drome, often paraneoplastic in origin, but reported in association with various infections. Little is known about adult-onset opsoclonus myoclonus syndrome (OMS) outside of individual case reports Objective: Describe a case of herpes-simplex virus 1 encephalitis presenting as opsoclonus-myoclonus ataxia Patients and methods: A 35 year-old woman, with no known comorbidities, developed a headache with nausea and vomiting, without fever or nuchal rigidity. In the following 48-hours, she presented an altered mental status, opsoclonus and myoclonus and was admitted to hospital. Lumbar puncture: 40 cells (60% mononu clear), protein 140 mg/dL and a normal glucose. Gram stain and culture for bacteria and fungi were negative. A PCR for herpes simplex virus was positive. Brain MRI: normal. Chest, Abdomen and Pelvis CT: no signs of neoplasia. Results: The patient received intra-venous acyclovir for 21 days, with resolution of symptoms Conclusion: OMS is an uncommon presentation of infections of central nervous system. Its fame extends further to the fact that OMS can be a harbinger of occult malignancy. The Adult-onset presentation is rare. Paraneoplastic and parainfectious causes (particularly virus) are common; however, more often OMS in adults occurs after systemic infection. After this report, HSV1 infection should be considered in OMS cases. We described the first case of OMS secondary to Herpes-Simplex Virus 1 infection.porreponame:Repositório Institucional da UFRNinstname:Universidade Federal do Rio Grande do Norte (UFRN)instacron:UFRNinfo:eu-repo/semantics/openAccessLICENSElicense.txtlicense.txttext/plain; charset=utf-81484https://repositorio.ufrn.br/bitstream/123456789/52559/2/license.txte9597aa2854d128fd968be5edc8a28d9MD52ORIGINALOpsoclonusmyoclonusSyndromeAssociated_Correia_Etal_2015.pdfOpsoclonusmyoclonusSyndromeAssociated_Correia_Etal_2015.pdfapplication/pdf39803https://repositorio.ufrn.br/bitstream/123456789/52559/1/OpsoclonusmyoclonusSyndromeAssociated_Correia_Etal_2015.pdf453b5d4fc8ea5f53da6f39604a40e1d0MD51123456789/525592023-05-29 14:24:18.406oai:https://repositorio.ufrn.br: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Repositório de PublicaçõesPUBhttp://repositorio.ufrn.br/oai/opendoar:2023-05-29T17:24:18Repositório Institucional da UFRN - Universidade Federal do Rio Grande do Norte (UFRN)false
dc.title.pt_BR.fl_str_mv Opsoclonus-myoclonus syndrome associated with herpes simplex encephalitis
title Opsoclonus-myoclonus syndrome associated with herpes simplex encephalitis
spellingShingle Opsoclonus-myoclonus syndrome associated with herpes simplex encephalitis
Afonso, C.O.M.
opsoclonus-myoclonus
encephalitis
paraneoplastic
title_short Opsoclonus-myoclonus syndrome associated with herpes simplex encephalitis
title_full Opsoclonus-myoclonus syndrome associated with herpes simplex encephalitis
title_fullStr Opsoclonus-myoclonus syndrome associated with herpes simplex encephalitis
title_full_unstemmed Opsoclonus-myoclonus syndrome associated with herpes simplex encephalitis
title_sort Opsoclonus-myoclonus syndrome associated with herpes simplex encephalitis
author Afonso, C.O.M.
author_facet Afonso, C.O.M.
Campos, M.L.S.
Maia, Ferdinand Gilbert Saraiva da Silva
Campêlo, C.L.C.
Camilo, A.F.C.
Correia, Carlos Eduardo Rocha
Fernandes, José Veríssimo
Figueiredo, Marcelo Marinho de
Silva, R.A.
author_role author
author2 Campos, M.L.S.
Maia, Ferdinand Gilbert Saraiva da Silva
Campêlo, C.L.C.
Camilo, A.F.C.
Correia, Carlos Eduardo Rocha
Fernandes, José Veríssimo
Figueiredo, Marcelo Marinho de
Silva, R.A.
author2_role author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Afonso, C.O.M.
Campos, M.L.S.
Maia, Ferdinand Gilbert Saraiva da Silva
Campêlo, C.L.C.
Camilo, A.F.C.
Correia, Carlos Eduardo Rocha
Fernandes, José Veríssimo
Figueiredo, Marcelo Marinho de
Silva, R.A.
dc.subject.por.fl_str_mv opsoclonus-myoclonus
encephalitis
paraneoplastic
topic opsoclonus-myoclonus
encephalitis
paraneoplastic
description Background: Opsoclonus-myoclonus ataxia is a rare neurologic syn drome, often paraneoplastic in origin, but reported in association with various infections. Little is known about adult-onset opsoclonus myoclonus syndrome (OMS) outside of individual case reports Objective: Describe a case of herpes-simplex virus 1 encephalitis presenting as opsoclonus-myoclonus ataxia Patients and methods: A 35 year-old woman, with no known comorbidities, developed a headache with nausea and vomiting, without fever or nuchal rigidity. In the following 48-hours, she presented an altered mental status, opsoclonus and myoclonus and was admitted to hospital. Lumbar puncture: 40 cells (60% mononu clear), protein 140 mg/dL and a normal glucose. Gram stain and culture for bacteria and fungi were negative. A PCR for herpes simplex virus was positive. Brain MRI: normal. Chest, Abdomen and Pelvis CT: no signs of neoplasia. Results: The patient received intra-venous acyclovir for 21 days, with resolution of symptoms Conclusion: OMS is an uncommon presentation of infections of central nervous system. Its fame extends further to the fact that OMS can be a harbinger of occult malignancy. The Adult-onset presentation is rare. Paraneoplastic and parainfectious causes (particularly virus) are common; however, more often OMS in adults occurs after systemic infection. After this report, HSV1 infection should be considered in OMS cases. We described the first case of OMS secondary to Herpes-Simplex Virus 1 infection.
publishDate 2015
dc.date.issued.fl_str_mv 2015-10-15
dc.date.accessioned.fl_str_mv 2023-05-29T17:23:27Z
dc.date.available.fl_str_mv 2023-05-29T17:23:27Z
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dc.identifier.citation.fl_str_mv CORREIA, Carlos Eduardo Rocha; et al. Opsoclonus-myoclonus syndrome associated with herpes simplex encephalitis. Journal Of The Neurological Sciences, [S.l.], v. 357, p. 56, out. 2015. Elsevier BV. Disponível em: https://www.sciencedirect.com/science/article/pii/S0022510X15007169?via%3Dihub. Acesso em: 29 mio 2023. DOI: http://dx.doi.org/10.1016/j.jns.2015.08.220
dc.identifier.uri.fl_str_mv https://repositorio.ufrn.br/handle/123456789/52559
dc.identifier.doi.none.fl_str_mv 10.1016/j.jns.2015.08.220.
identifier_str_mv CORREIA, Carlos Eduardo Rocha; et al. Opsoclonus-myoclonus syndrome associated with herpes simplex encephalitis. Journal Of The Neurological Sciences, [S.l.], v. 357, p. 56, out. 2015. Elsevier BV. Disponível em: https://www.sciencedirect.com/science/article/pii/S0022510X15007169?via%3Dihub. Acesso em: 29 mio 2023. DOI: http://dx.doi.org/10.1016/j.jns.2015.08.220
10.1016/j.jns.2015.08.220.
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dc.publisher.none.fl_str_mv Journal Of The Neurological Sciences
publisher.none.fl_str_mv Journal Of The Neurological Sciences
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